Clinical Research Associate - Oncology

Responsibilities

• Conduct on-site and remote monitoring visits, ensuring adherence to protocol, GCP, and regulatory requirements
• Manage site relationships, including issue escalation, conflict resolution, and performance oversight
• Review and verify clinical data, including source documentation, EDC entries, and key performance metrics (DOS, TMS timelines, report turnaround)
• Identify and resolve site issues, including protocol deviations, CAPAs, and systemic vs. isolated concerns
• Ensure investigational product (IP) accountability and perform reconciliation, including discrepancy resolution

Requirements

• 3+ years of experience with on-site monitoring as a Clinical Research Associate
• Strong oncology expertise, including knowledge of RECIST, ECOG performance status, CTCAE grading, and dosing concepts
• Proven ability to manage multiple priorities, work independently, and support multiple sponsors simultaneously

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, or a related field

Compensation

Salary Range: [$120,000 – $180,000] depending on experience
Full Benefits Package: PTO, Paid Holidays, Medical, Dental, Vision, 401K, Tuition Reimbursement, Sick leave as required by law